Pharmacovigilance Associate

Airvin Skills; Hyderabad, Mysuru, Bengaluru; On-site; INR 180,000 - 240,000; Full time

Job summary

Airvin Skills is seeking a motivated Entry-Level Pharmacovigilance Associate to support adverse event case processing, data management, and regulatory compliance. The role offers hands-on training in drug safety and exposure to global pharmacovigilance practices.

As a recent graduate with a keen eye for detail, you will enter and manage case data, generate data summaries, and assist senior staff in regulatory submissions.

Qualifications

• Bachelor's degree in Pharmacy, Pharmacology, Life Sciences, Nursing, or related field.
• Recent graduate with strong interest in drug safety.
• Excellent attention to detail and accuracy.
• Strong organizational and time-management skills.
• Proficient in MS Office (Word, Excel, PowerPoint).
• Ability to work independently and in a team.
• Good communication and interpersonal skills.

Responsibilities

• Enter and triage adverse event reports into the PV database.
• Assist in preparation of safety reports and data summaries.
• Follow SOPs and regulatory guidelines for data entry and case processing.
• Support maintenance of PV databases and records.
• Participate in team meetings and training sessions.

Skills

Attention to detail

Time management

Communication skills

Teamwork

Independent work

Education

Bachelor's degree in Pharmacy/Pharmacology/Life Sciences

Tools

Microsoft Office

Job description

We are seeking a highly motivated and detail-oriented recent graduate to join our Pharmacovigilance team as an Entry-Level Pharmacovigilance Associate. This is a fantastic opportunity to begin your career in the pharmaceutical industry and contribute to the safety monitoring of our products. You will gain hands-on experience in various aspects of pharmacovigilance, including adverse event reporting, data entry, and case processing. This role is ideal for individuals with a strong interest in drug safety and a desire to learn and grow in a dynamic environment.

Responsibilities:

Adverse Event Case Processing:

• Receive, triage, and accurately enter adverse event reports into the pharmacovigilance database.
• Ensure timely and accurate data entry according to company Standard Operating Procedures (SOPs) and regulatory guidelines.
• Assist in the follow-up of adverse event reports to obtain complete information.
• Perform quality checks on case data to ensure accuracy and consistency.

Data Management and Reporting:

• Assist in the preparation of safety reports and data summaries.
• Maintain accurate and organized pharmacovigilance records.
• Assist in the tracking and monitoring of adverse event trends.

Regulatory Compliance:

• Gain a basic understanding of global pharmacovigilance regulations and guidelines.
• Adhere to company SOPs and regulatory requirements.
• Assist in the preparation of regulatory submissions.

General Support:

• Assist in the maintenance of pharmacovigilance databases and systems.
• Participate in team meetings and training sessions.
• Support senior pharmacovigilance staff as needed.
• Any other duties as assigned.

Qualifications:

• Bachelor's degree in Pharmacy, Pharmacology, Life Sciences, Nursing, or a related healthcare field.
• Strong interest in drug safety and pharmacovigilance.
• Excellent attention to detail and accuracy.
• Strong organizational and time-management skills.
• Ability to work independently and as part of a team.
• Good communication and interpersonal skills.
• Proficiency in Microsoft Office Suite ("Word, Excel, PowerPoint").
• Must be a recent graduate.